Retinoschisis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1137478
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Genes

20 genes associated with the disease Retinoschisis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
ACTG1 actin gamma 1
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
ATP1B2 ATPase, Na+/K+ transporting, beta 2 polypeptide
CDKL5 cyclin-dependent kinase-like 5
COL2A1 collagen, type II, alpha 1
CRB1 crumbs family member 1, photoreceptor morphogenesis associated
DMD dystrophin
ERG v-ets avian erythroblastosis virus E26 oncogene homolog
FNDC3A fibronectin type III domain containing 3A
MBTPS2 membrane-bound transcription factor peptidase, site 2
NR2E3 nuclear receptor subfamily 2, group E, member 3
PHEX phosphate regulating endopeptidase homolog, X-linked
PLXNA2 plexin A2
PPEF1 protein phosphatase, EF-hand calcium binding domain 1
RAX retina and anterior neural fold homeobox
RPE ribulose-5-phosphate-3-epimerase
RPGR retinitis pigmentosa GTPase regulator
RS1 retinoschisin 1
RSC1A1 regulatory solute carrier protein, family 1, member 1